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Clinical Trials/NCT01126320
NCT01126320
Completed
Not Applicable

Frequency of Ventilator Associated Pneumonia (VAP) in Mechanically Ventilated ICU Patients Using the AnapnoGuard System

Hospitech Respiration1 site in 1 country161 target enrollmentDecember 2010

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Ventilator Associated Pneumonia
Sponsor
Hospitech Respiration
Enrollment
161
Locations
1
Primary Endpoint
VAP occurence
Status
Completed
Last Updated
10 years ago

Overview

Brief Summary

Ventilator Associated Pneumonia (VAP) is a common complication experienced by mechanically ventilated patients and within the framework of Respiratory Intensive Care Units. The AnapnoGuard system, developed by Hospitech Respiration Ltd. is a ventilation guard system that includes a number of unique characteristics. This study was designed to test the frequency VAP in mechanically ventilated ICU patients using the AnapnoGuard System.

Registry
clinicaltrials.gov
Start Date
December 2010
End Date
December 2015
Last Updated
10 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Hospitech Respiration
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • ICU patients;
  • Patient was connected to AnapnoGuard system up to six hours from intubation;
  • Age - above 18.

Exclusion Criteria

  • Pneumonia;
  • Aspiration Pneumonia;
  • Chronic or Severe Pneumonia;
  • Chronic Obstructive Pulmonary Disease (COPD) requiring permanent home-based antibiotic treatment;
  • Interstitial Lung Disease (ILD);
  • Post Lung Transplant State;
  • Immunosuppression.
  • Patients ventilated in prone position
  • Patient who was ventilated 3 months prior to being enrolled in the study
  • Pregnant women

Outcomes

Primary Outcomes

VAP occurence

Time Frame: 2 years

Secondary Outcomes

  • Adverse events occurence(2 years)

Study Sites (1)

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